Actelion has announced the initiation of the Phase III program, Conscious-2, for the endothelin receptor antagonist Pivlaz. The study is designed to evaluate the safety and efficacy of Pivlaz in reducing vasospasm-related morbidity and all-cause mortality following aneurysmal subarachnoid hemorrhage.
Subscribe to our email newsletter
Conscious-2 is a global study, and will include a minimum of 765 patients from more than 100 centers, randomized 2:1 to receive either 5mg/h of Pivlaz (clazosentan) or placebo. Conscious-2 will subsequently measure the clinical benefits of Pivlaz through the primary endpoint of vasospasm-related morbidity and all-cause mortality which includes neurological deterioration, new brain infarcts, introduction of vasospasm rescue therapy or death from any cause. The Conscious-2 trial will also investigate the effect of Pivlaz on the extended Glasgow outcomes scale (GOSE) at three month as a secondary endpoint.
In earlier studies, the use of Pivlaz was associated with up to 65% reduction in vasospasm, a contraction of blood vessels in the brain.
Neal Kassell, chairman of the Conscious-2 Steering Committee (Clazosentan to overcome neurological iSChemia and Infarct occUrring after subarachnoid hemorrhage), said: “Vasospasm is a major problem in patients with aneurysmal subarachnoid hemorrhage. Vasospasm is both unpredictable and the leading treatable cause of disability and death. A reduction in the occurrence of vasospasm is expected to result in measurable clinical benefit. The Conscious-2 trial is specifically designed to demonstrate this benefit.”
Advertise With UsAdvertise on our extensive network of industry websites and newsletters.
Get the PBR newsletterSign up to our free email to get all the latest PBR
news.